Package 41250-219-05

Brand: sinus severe

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 41250-219-05
Digits Only 4125021905
Product NDC 41250-219
Description

2 BLISTER PACK in 1 CARTON (41250-219-05) / 12 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-09-30
Brand sinus severe
Generic acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24348985-5afc-8f40-e063-6294a90a587b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0708820130692"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["8504bb16-4ad7-2732-e053-2991aa0affd1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (41250-219-05)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "41250-219-05", "marketing_end_date": "20260930", "marketing_start_date": "20170401"}], "brand_name": "sinus severe", "product_id": "41250-219_24348985-5afc-8f40-e063-6294a90a587b", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "41250-219", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Meijer", "product_type": "HUMAN OTC DRUG", "brand_name_base": "sinus severe", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260930", "marketing_start_date": "20170401"}